HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 375387Generated: October 25, 2026
Dimethylformamide → 2-Difluoroacetylimino-3(3-trifluoromethylphenyl)-5-methylthiazoline
https://huagongshe.com/reaction/375387
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | Tetrafluoroethylene | HCID 8301 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Imino-3-(3-trifluoromethyl-phenyl)-5-methylthiazoline hydrochloride | HCID 21480071 | — |
| Product | 2-Difluoroacetylimino-3(3-trifluoromethylphenyl)-5-methylthiazoline | HCID 11088983 | 93% |
Reaction Steps
A solution of 2-imino-3-(3-trifluoromethylphenyl)-5-methylthiazoline hydrochloride (1.47 g, 5.0 mmol), piperidine (0.64 g, 7.5 mmol) and triethylamine (1.77 g, 17.5 mmol) in N,N-dimethylformamide (10 ml) charged in a reaction flask was reacted with tetrafluoroethylene, which was made to flow intothe flask (ca. 0.7 liter/hr), with vigorous stirring at 50° C. for 13 hours. After cooling to an ambient temperature, the reaction mixture was poured into ice-water, and extracted with diethyl ether. The ether layer was washed with water and then brine, and dried over anhydrous magnesium sulfate. The solvent was distilled off, and the residue was subjected to silica gel column chromatography, which afforded 2-difluoroacetylimino-3-(3-trifluoromethylphenyl)-5-methylthiazoline (1.56 g, 4.6 mmol, yield 93%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05484933 |
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| Source dataset | uspto-grants-1996_01 |
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| ORD ID | ord-eb7097af06cb4b64ba302a0a1fee4136 |
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| Source note | uspto-grants-1996_01 |
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